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Trait
Cervical spine instability
An abnormal lack of stability of the cervical spine.
Summary
- Body system
- Abnormality of the musculoskeletal system
Cervical spine instabilityHP:0010646
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Read the genes linked to Cervical spine instability, and the rest of your genome, with one test.
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Get my Genome Test10 genes linked to Cervical spine instability
Changes in these genes cause rare conditions in which Cervical spine instability is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| POP1POP1 ribonuclease P/MRP subunit | Always | In 1 condition |
| SOX9SRY-box transcription factor 9 | Always | In 1 condition |
| B3GALT6beta-1,3-galactosyltransferase 6 | Often (30–79%) | In 2 conditions |
| COL2A1collagen type II alpha 1 chain | Often (30–79%) | In 1 condition |
| ARSLarylsulfatase L | Sometimes (5–29%) | In 1 condition |
| TGFBR1transforming growth factor beta receptor 1 | Sometimes (5–29%) | In 1 condition |
| COMPcartilage oligomeric matrix protein | Rarely (1–4%) | In 1 condition |
| SMAD3SMAD family member 3 | Rarely (1–4%) | In 1 condition |
| TGFB3transforming growth factor beta 3 | Rarely (1–4%) | In 1 condition |
| BGNbiglycan | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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